Page last updated: 2024-12-05

indican

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Indican is a naturally occurring compound found in plants, particularly in the indigo plant (Indigofera tinctoria). It is a colorless glycoside that breaks down into indigo, a blue dye, upon exposure to air or enzymatic hydrolysis. Indican itself does not have any significant pharmacological effects. It is primarily studied for its role in the production of indigo, which has been used for centuries as a dye and has also been investigated for its potential antioxidant and antimicrobial properties. The synthesis of indican involves the enzymatic conversion of tryptophan to indoxyl, followed by conjugation with glucose. Upon hydrolysis, indican releases indoxyl, which then oxidizes to indigo. While indican is not directly responsible for any specific effects, its breakdown product, indigo, is being explored for its potential applications in various fields.'

indoxyl sulfate : An aryl sulfate that is indoxyl in which the hydroxyl hydrogen is substituted by a sulfo group. [Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Cross-References

ID SourceID
PubMed CID441564
CHEMBL ID2063300
CHEBI ID16700
SCHEMBL ID15756
MeSH IDM0011222
PubMed CID10258
CHEMBL ID1233636
CHEBI ID43355
SCHEMBL ID15755
MeSH IDM0011222

Synonyms (82)

Synonym
3-indolyl-beta-d-glucopyranoside
CHEBI:16700 ,
1h-indol-3-yl beta-d-glucopyranoside
SMP2_000304
nsc-87517
indoxyl beta-d-glucoside
487-60-5
indican ,
indoxyl beta-d-glucoside, bioxtra, >=97%
indoxyl beta-d-glucoside, >=97%
2-(hydroxymethyl)-6-(1h-indol-3-yloxy)tetrahydropyran-3,4,5- triol
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(1h-indol-3-yloxy)oxane-3,4,5-triol
3-indoxyl-beta-d-glucopyranoside
beta-d-glucopyranoside, 1h-indol-3-yl
n187wk1y1j ,
indole, 3-(beta-d-glucopyranosyloxy)-
unii-n187wk1y1j
1h-indol-3-yl beta-glucopyranoside
nsc 87517
3-(glucosyloxy)indole
CHEMBL2063300
1h-indol-3-yl-.beta.-d-glucopyranoside
indican [mi]
SCHEMBL15756
indican-reaktion
AKOS016844826
3-indolyl-b-d-glucopyranoside
XVARCVCWNFACQC-RKQHYHRCSA-N
mfcd00047169
AS-59844
indoxyl beta-d-glucoside, vetec(tm) reagent grade, 97%
DTXSID10903997
Q418392
(2r,3s,4s,5r,6s)-2-(hydroxymethyl)-6-(1h-indol-3-yloxy)tetrahydropyran-3,4,5-triol
(2s,3r,4s,5s,6r)-2-(1h-indol-3-yloxy)-6-(hydroxymethyl)tetrahydro-2h-pyran-3,4,5-triol
(2s,3r,4s,5s,6r)-2-((1h-indol-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2h-pyran-3,4,5-triol
indoxyl ?-glucoside
indoxylbeta-d-glucoside
HY-122009
indoxyl beta -d-glucoside
3-(beta-d-glucosido)indole, plant indican
A871882
CS-0078782
CHEMBL1233636 ,
chebi:43355 ,
3-sulfooxy-1h-indole
IOS ,
indoxyl sulfate
3-indolyl hydrogen sulfate
3-indoxylsulfuric acid
3-indolyl sulfate
indoxyl sulphate
DB07992
indoxyl-3-sulphate
indoxylsulfuric acid
indoxyl sulfic acid
indol-3-yl hydrogen sulfate
indol-3-yl sulfate
1h-indol-3-yl hydrogen sulfate
3-indoxyl sulfate
kt0qa88913 ,
indican (metabolic indolyl sulfate)
unii-kt0qa88913
487-94-5
1h-indol-3-ol, hydrogen sulfate (ester)
indican (metabolic indican)
bdbm50420185
indol-3-yl sulphate
SCHEMBL15755
1h-indol-3-ol, 3-(hydrogen sulfate)
indoxyl sulfate [mi]
BXFFHSIDQOFMLE-UHFFFAOYSA-N
1h-indol-3-yloxidanesulfonic acid
indoxylsulfate
1h-indol-3-yl hydrogen sulphate
3-indoxyl sulphate
Q11712146
EN300-1268263
(1h-indol-3-yl)oxidanesulfonic acid
1h-indol-3-ylhydrogensulfate
DTXSID701043787
AKOS040752080

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" It is concluded that some of the protein binding inhibitors have toxic effects on cell function of various tissues and play a role in pathophysiology of uremia."( [Study on the uremic protein binding inhibitors as uremic toxin: toxic effect on erythroid colony formation, lymphocyte blast formation and renal function].
Kawashima, Y, 1989
)
0.28
" A progressive decline in the glomerular filtration rate leads to increased serum levels of endogenous protein metabolites such as indoxyl sulfate, and to the adverse effects of their overload on the remnant nephrons."( Uremic toxicity of indoxyl sulfate.
Niwa, T, 2010
)
0.36
" Studies have suggested that indoxyl sulfate also has adverse effects on bones and the central nervous system."( Indoxyl Sulfate-Review of Toxicity and Therapeutic Strategies.
Leong, SC; Sirich, TL, 2016
)
0.43
"Recently, the clinical and experimental evidences that support the toxic effects of indoxyl sulfate, a protein-bound uremic toxin in chronic kidney disease (CKD) patients, has been discussed."( Comment on Indoxyl Sulfate-Review of Toxicity and Therapeutic Strategies. Toxins 2016, 8, 358.
Barreto, DV; Barreto, FC; Massy, ZA; Stinghen, AEM, 2017
)
0.46
" Furthermore, adverse events including electrolyte abnormalities were not observed."( Safety and efficacy of using cereal food (Frugra®) to improve blood pressure and bowel health in patients undergoing chronic hemodialysis: A pilot study.
Amano, A; Dohi, T; Fukushima, Y; Kaifu, K; Kasai, T; Kobayashi, T; Matsushita, S; Nagasawa, H; Okuma, T; Ono, S; Otsuka, T; Suzuki, Y; Ueda, S, 2021
)
0.62
" The aryl hydrocarbon receptor (AhR) is a ligand-activated transcription factor that regulates the toxic effects of uremic toxins."( Toxic Effects of Indoxyl Sulfate on Osteoclastogenesis and Osteoblastogenesis.
Chang, CT; Chen, YC; Fang, TC; Hou, YC; Liao, TY; Liu, WC; Lu, KC; Shyu, JF; Zheng, CM, 2021
)
0.62

Pharmacokinetics

ExcerptReferenceRelevance
"The purpose of the present study was to examine the pharmacokinetic properties of indoxyl sulphate, a harmful uraemic toxin that accumulates during chronic renal failure."( Pharmacokinetics and tissue distribution of uraemic indoxyl sulphate in rats.
Deguchi, T; Nakamura, M; Otagiri, M; Suenaga, A; Tsutsumi, Y, 2003
)
0.32
" Route-randomized, two-way crossover pharmacokinetic studies of ER were conducted in 12 ESRD patients and 12 healthy controls after oral (250 mg) and intravenous (125 mg) dosing with ER."( Hepatic clearance, but not gut availability, of erythromycin is altered in patients with end-stage renal disease.
Benet, LZ; Frassetto, LA; Huang, Y; Sun, H, 2010
)
0.36
"The 5/6 nephrectomized (5/6 Nx) rat model, to simulate chronic renal failure (CRF) patients, combined with kidney slices and transporter studies in vitro were used to assess this pharmacokinetic differences."( Mechanistic Study on the Effect of Renal Impairment on the Pharmacokinetics of Vildagliptin and its Carboxylic Acid Metabolite.
Chen, X; Chen, Z; Guo, Z; Hu, J; Kong, F; Xie, N, 2022
)
0.72

Compound-Compound Interactions

ExcerptReferenceRelevance
" Moreover, more information can be provided on the evaluation of toxicity of phorate using metabonomics combined with clinical chemistry."( Metabonomics evaluation of urine from rats administered with phorate under long-term and low-level exposure by ultra-performance liquid chromatography-mass spectrometry.
Guo, L; Hou, Y; Sun, C; Sun, X; Xu, W; Zeng, Y; Zhao, X, 2014
)
0.4

Bioavailability

ExcerptReferenceRelevance
" With oral dosing, the bioavailability of ER increased 36% in patients with ESRD, and this increase was not related to changes in gut availability."( Hepatic clearance, but not gut availability, of erythromycin is altered in patients with end-stage renal disease.
Benet, LZ; Frassetto, LA; Huang, Y; Sun, H, 2010
)
0.36

Dosage Studied

ExcerptRelevanceReference
"5%) for 6 weeks excreted increased amounts of p-cresol, but many excreted negligible amounts so that the overall dose-response relationship was bell shaped."( The effect of saccharin ingestion on the excretion of microbial amino acid metabolites in rat and man.
Lawrie, CA; Renwick, AG, 1987
)
0.27
" Route-randomized, two-way crossover pharmacokinetic studies of ER were conducted in 12 ESRD patients and 12 healthy controls after oral (250 mg) and intravenous (125 mg) dosing with ER."( Hepatic clearance, but not gut availability, of erythromycin is altered in patients with end-stage renal disease.
Benet, LZ; Frassetto, LA; Huang, Y; Sun, H, 2010
)
0.36
"CKD rats were produced by 5/6 nephrectomy and were divided into 2 groups: (1) CKD rats and (2) AST-120-treated CKD rats at a dosage of 4 g/kg body weight/day."( AST-120 ameliorates epithelial-to-mesenchymal transition and interstitial fibrosis in the kidneys of chronic kidney disease rats.
Bolati, D; Niwa, T; Shimizu, H, 2012
)
0.38
" A quality score was developed, giving 1 point for each of the following criteria: six or more experiments, confirmation by more than one experimental approach, neutralization of the biologic effect by counteractive reagents or antibodies, use of a real-life model, and use of dose-response analyses in vitro and/or animal studies."( The uremic toxicity of indoxyl sulfate and p-cresyl sulfate: a systematic review.
Glorieux, G; Nagler, EV; Pletinck, A; Schepers, E; Vanholder, R, 2014
)
0.4
" The uptake of liposomes by direct incubation in vitro showed an obvious dose-response relationship for p-cresyl sulfate (PCS) and indoxyl sulfate (IS) but not for hippuric acid (HA)."( Increasing the removal of protein-bound uremic toxins by liposome-supported hemodialysis.
Ding, F; Li, Y; Liu, T; Ma, S; Shi, Y; Tian, H; Wang, W; Wang, Y; Zhu, Q, 2019
)
0.51
" We treated six dogs with a 1-g/kg/day oral dosage of AST-120 for 14 days from week 4 after the start of rapid ventricular pacing."( AST-120, an Adsorbent of Uremic Toxins, Improves the Pathophysiology of Heart Failure in Conscious Dogs.
Asakura, M; Asano, Y; Asanuma, H; Chung, H; Fukuda, H; Funayama, M; Ihara, M; Imazu, M; Ito, S; Kitakaze, M; Min, KD; Minamino, T; Morita, T; Ogai, A; Sugimachi, M; Takahama, H; Takashima, S, 2019
)
0.51
" The total and free serum concentration of p-cresyl sulfate (PCS), indoxyl sulfate (IS) and indole-3-acetic acid (IAA) were dosed by high-performance liquid chromatography."( Influence of bowel habits on gut-derived toxins in peritoneal dialysis patients.
Cuppari, L; Dalboni, MA; de Andrade, LS; de Lima, JD; Nakao, LS; Pereira, NBF; Ramos, CI; Rodrigues, SD; Teixeira, RR, 2020
)
0.56
" In conclusion, the limited data reported in this present study indicates that monitoring IS in the blood is a very important determinant in the dosage plan for the administration of site II drugs such as ARP, if the efficacy of the drug in renal disease is to be considered."( The Binding of Aripiprazole to Plasma Proteins in Chronic Renal Failure Patients.
Chuang, VTG; Hirata, K; Ikeda, T; Maruyama, T; Nishi, K; Otagiri, M; Sakurama, K; Tanaka, M; Uchida, Y; Watanabe, H; Yamasaki, K, 2021
)
0.62
" Restricted cubic spline model was performed to assess dose-response relationships between tIS concentration and all-cause and CVD mortality."( Serum total indoxyl sulfate levels and all-cause and cardiovascular mortality in maintenance hemodialysis patients: a prospective cohort study.
Jiang, BW; Jin, YX; Li, Q; Liu, SX; Mu, XW; Song, JN; Wang, SN; Wang, XN; Wang, ZH; Wang, ZZ; Wu, QJ; Xiao, J; Yan, XY; You, LL; Zhang, S; Zhang, Y; Zhao, XN, 2022
)
0.72
" For 137 sessions, in 36 patients the total daily dosage of UV-absorbing drugs was less than 500 mg, and for 6 sessions 3 patients received additional UV-absorbing drugs."( Treatment with Paracetamol Can Interfere with the Intradialytic Optical Estimation in Spent Dialysate of Uric Acid but Not of Indoxyl Sulfate.
Adoberg, A; Arund, J; Dhondt, A; Fridolin, I; Glorieux, G; Holmar, J; Lauri, K; Leis, L; Luman, M; Paats, J; Pilt, K; Tanner, R; Uhlin, F, 2022
)
0.72
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
human metaboliteAny mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens).
[role information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Drug Classes (5)

ClassDescription
indolyl carbohydrate
beta-D-glucosideAny D-glucoside in which the anomeric centre has beta-configuration.
exopolysaccharideA biomacromolecule composed of carbohydrate residues which is secreted by a microorganism into the surrounding environment.
indolesAny compound containing an indole skeleton.
aryl sulfate
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Pathways (2)

PathwayProteinsCompounds
indican biosynthesis010
indican biosynthesis011
Tryptophan metabolism2342

Protein Targets (5)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Solute carrier family 22 member 6Homo sapiens (human)IC50 (µMol)83.00000.27004.53069.9000AID682036
Solute carrier family 22 member 6Homo sapiens (human)Ki22.85000.03003.20437.8200AID679369; AID679400
Solute carrier family 22 member 8Homo sapiens (human)Ki168.85000.04004.22979.0000AID681029; AID681043
Solute carrier family 22 member 11Homo sapiens (human)Ki181.15000.20002.57716.1500AID680180; AID681674
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Activation Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Other Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Solute carrier family 22 member 6Homo sapiens (human)Km21.00000.42004.61839.3000AID678998
Solute carrier family 22 member 8Homo sapiens (human)Km263.00000.34501.32173.1000AID679675
Solute carrier family 22 member 8Rattus norvegicus (Norway rat)Km166.00000.73901.53952.3400AID679631; AID681222
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (18)

Processvia Protein(s)Taxonomy
cellular response to starvationAlbuminBos taurus (cattle)
negative regulation of mitochondrial depolarizationAlbuminBos taurus (cattle)
cellular response to calcium ion starvationAlbuminBos taurus (cattle)
monoatomic anion transportSolute carrier family 22 member 6Homo sapiens (human)
response to organic cyclic compoundSolute carrier family 22 member 6Homo sapiens (human)
inorganic anion transportSolute carrier family 22 member 6Homo sapiens (human)
organic anion transportSolute carrier family 22 member 6Homo sapiens (human)
prostaglandin transportSolute carrier family 22 member 6Homo sapiens (human)
alpha-ketoglutarate transportSolute carrier family 22 member 6Homo sapiens (human)
xenobiotic transportSolute carrier family 22 member 6Homo sapiens (human)
sodium-independent organic anion transportSolute carrier family 22 member 6Homo sapiens (human)
transmembrane transportSolute carrier family 22 member 6Homo sapiens (human)
metanephric proximal tubule developmentSolute carrier family 22 member 6Homo sapiens (human)
renal tubular secretionSolute carrier family 22 member 6Homo sapiens (human)
monoatomic ion transportSolute carrier family 22 member 8Homo sapiens (human)
response to toxic substanceSolute carrier family 22 member 8Homo sapiens (human)
inorganic anion transportSolute carrier family 22 member 8Homo sapiens (human)
prostaglandin transportSolute carrier family 22 member 8Homo sapiens (human)
xenobiotic transportSolute carrier family 22 member 8Homo sapiens (human)
transmembrane transportSolute carrier family 22 member 8Homo sapiens (human)
transport across blood-brain barrierSolute carrier family 22 member 8Homo sapiens (human)
monoatomic ion transportSolute carrier family 22 member 11Homo sapiens (human)
inorganic anion transportSolute carrier family 22 member 11Homo sapiens (human)
organic anion transportSolute carrier family 22 member 11Homo sapiens (human)
prostaglandin transportSolute carrier family 22 member 11Homo sapiens (human)
urate metabolic processSolute carrier family 22 member 11Homo sapiens (human)
transmembrane transportSolute carrier family 22 member 11Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (18)

Processvia Protein(s)Taxonomy
oxygen bindingAlbuminBos taurus (cattle)
DNA bindingAlbuminBos taurus (cattle)
fatty acid bindingAlbuminBos taurus (cattle)
protein bindingAlbuminBos taurus (cattle)
toxic substance bindingAlbuminBos taurus (cattle)
pyridoxal phosphate bindingAlbuminBos taurus (cattle)
metal ion bindingAlbuminBos taurus (cattle)
enterobactin bindingAlbuminBos taurus (cattle)
solute:inorganic anion antiporter activitySolute carrier family 22 member 6Homo sapiens (human)
protein bindingSolute carrier family 22 member 6Homo sapiens (human)
organic anion transmembrane transporter activitySolute carrier family 22 member 6Homo sapiens (human)
prostaglandin transmembrane transporter activitySolute carrier family 22 member 6Homo sapiens (human)
alpha-ketoglutarate transmembrane transporter activitySolute carrier family 22 member 6Homo sapiens (human)
antiporter activitySolute carrier family 22 member 6Homo sapiens (human)
transmembrane transporter activitySolute carrier family 22 member 6Homo sapiens (human)
chloride ion bindingSolute carrier family 22 member 6Homo sapiens (human)
identical protein bindingSolute carrier family 22 member 6Homo sapiens (human)
xenobiotic transmembrane transporter activitySolute carrier family 22 member 6Homo sapiens (human)
sodium-independent organic anion transmembrane transporter activitySolute carrier family 22 member 6Homo sapiens (human)
solute:inorganic anion antiporter activitySolute carrier family 22 member 8Homo sapiens (human)
organic anion transmembrane transporter activitySolute carrier family 22 member 8Homo sapiens (human)
prostaglandin transmembrane transporter activitySolute carrier family 22 member 8Homo sapiens (human)
xenobiotic transmembrane transporter activitySolute carrier family 22 member 8Homo sapiens (human)
solute:inorganic anion antiporter activitySolute carrier family 22 member 11Homo sapiens (human)
protein bindingSolute carrier family 22 member 11Homo sapiens (human)
organic anion transmembrane transporter activitySolute carrier family 22 member 11Homo sapiens (human)
prostaglandin transmembrane transporter activitySolute carrier family 22 member 11Homo sapiens (human)
sodium-independent organic anion transmembrane transporter activitySolute carrier family 22 member 11Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (10)

Processvia Protein(s)Taxonomy
extracellular regionAlbuminBos taurus (cattle)
extracellular spaceAlbuminBos taurus (cattle)
protein-containing complexAlbuminBos taurus (cattle)
plasma membraneSolute carrier family 22 member 6Homo sapiens (human)
caveolaSolute carrier family 22 member 6Homo sapiens (human)
basal plasma membraneSolute carrier family 22 member 6Homo sapiens (human)
basolateral plasma membraneSolute carrier family 22 member 6Homo sapiens (human)
extracellular exosomeSolute carrier family 22 member 6Homo sapiens (human)
protein-containing complexSolute carrier family 22 member 6Homo sapiens (human)
plasma membraneSolute carrier family 22 member 8Homo sapiens (human)
basolateral plasma membraneSolute carrier family 22 member 8Homo sapiens (human)
apical plasma membraneSolute carrier family 22 member 8Homo sapiens (human)
extracellular exosomeSolute carrier family 22 member 8Homo sapiens (human)
plasma membraneSolute carrier family 22 member 11Homo sapiens (human)
external side of plasma membraneSolute carrier family 22 member 11Homo sapiens (human)
basal plasma membraneSolute carrier family 22 member 11Homo sapiens (human)
apical plasma membraneSolute carrier family 22 member 11Homo sapiens (human)
extracellular exosomeSolute carrier family 22 member 11Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (41)

Assay IDTitleYearJournalArticle
AID674374Cytotoxicity against human MCF7 cells at 10 uM after 96 hrs by MTT assay2012Journal of natural products, Jun-22, Volume: 75, Issue:6
Alkaloids from the root of Isatis indigotica.
AID674375Cytotoxicity against human Bel7402 cells at 10 uM after 96 hrs by MTT assay2012Journal of natural products, Jun-22, Volume: 75, Issue:6
Alkaloids from the root of Isatis indigotica.
AID674372Cytotoxicity against human A549 cells at 10 uM after 96 hrs by MTT assay2012Journal of natural products, Jun-22, Volume: 75, Issue:6
Alkaloids from the root of Isatis indigotica.
AID674376Cytotoxicity against human Ketr3 cells at 10 uM after 96 hrs by MTT assay2012Journal of natural products, Jun-22, Volume: 75, Issue:6
Alkaloids from the root of Isatis indigotica.
AID674373Cytotoxicity against human BGC823 cells at 10 uM after 96 hrs by MTT assay2012Journal of natural products, Jun-22, Volume: 75, Issue:6
Alkaloids from the root of Isatis indigotica.
AID674370Antiviral activity against HIV1 infected in 293T cells cotransfected with VSV-G at 10 uM after 48 hrs by ELISA2012Journal of natural products, Jun-22, Volume: 75, Issue:6
Alkaloids from the root of Isatis indigotica.
AID674371Antiviral activity against Herpes simplex virus 1 at 10 uM2012Journal of natural products, Jun-22, Volume: 75, Issue:6
Alkaloids from the root of Isatis indigotica.
AID674377Cytotoxicity against human HCT8 cells at 10 uM after 96 hrs by MTT assay2012Journal of natural products, Jun-22, Volume: 75, Issue:6
Alkaloids from the root of Isatis indigotica.
AID1624942Stability of the compound in pH 7 ammonium acetate buffer by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID1624948Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis by measuring catalytic efficiency by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID681674TP_TRANSPORTER: uptake&inhibition of estrone sulfate in OAT4-S2 cells2003European journal of pharmacology, Apr-11, Volume: 466, Issue:1-2
Interactions of human organic anion as well as cation transporters with indoxyl sulfate.
AID1624939Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis using 1 U of enzyme measured after 20.5 hrs by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID679369TP_TRANSPORTER: uptake&inhibition of PAH in OAT1-S2 cells2003European journal of pharmacology, Apr-11, Volume: 466, Issue:1-2
Interactions of human organic anion as well as cation transporters with indoxyl sulfate.
AID682034TP_TRANSPORTER: transepithelial transport of erythromycin in the presence of Indoxyl sulfate at 1mM in MDR1-expressing MDCK cells2004Drug metabolism and disposition: the biological fate of chemicals, Nov, Volume: 32, Issue:11
Effects of uremic toxins on hepatic uptake and metabolism of erythromycin.
AID1624938Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis using 0.1 U of enzyme by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID1324533Binding affinity to BSA assessed as dissociation rate constants of the ligand-target complex at 2 mM in presence of 0.06 mM L-tryptophan by (1)H relaxation dispersion NMR spectroscopy2016Journal of medicinal chemistry, 12-08, Volume: 59, Issue:23
Measurement of Ligand-Target Residence Times by
AID679400TP_TRANSPORTER: inhibition of PAH uptake (PAH: 5 uM, indoxyl sulfate:500 uM) in S2 human-OAT1 expressing cells2003European journal of pharmacology, Apr-11, Volume: 466, Issue:1-2
Interactions of human organic anion as well as cation transporters with indoxyl sulfate.
AID679675TP_TRANSPORTER: uptake in OAT3-expressing HEK293 cells2004Kidney international, Jan, Volume: 65, Issue:1
Characterization of uremic toxin transport by organic anion transporters in the kidney.
AID681029TP_TRANSPORTER: uptake&inhibition of estrone sulfate in OAT3-S2 cells2003European journal of pharmacology, Apr-11, Volume: 466, Issue:1-2
Interactions of human organic anion as well as cation transporters with indoxyl sulfate.
AID681168TP_TRANSPORTER: uptake in Oat3-expressing oocyte cells2004The Journal of pharmacology and experimental therapeutics, Jun, Volume: 309, Issue:3
Mouse reduced in osteosclerosis transporter functions as an organic anion transporter 3 and is localized at abluminal membrane of blood-brain barrier.
AID681222TP_TRANSPORTER: uptake in Xenopus laevis oocytes2002Kidney international, May, Volume: 61, Issue:5
Major role of organic anion transporter 3 in the transport of indoxyl sulfate in the kidney.
AID1624940Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis using 5 U of enzyme by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID682036TP_TRANSPORTER: inhibition of PAH uptake in OAT-expressing OK cells2002British journal of pharmacology, Jan, Volume: 135, Issue:2
Uraemic toxins induce proximal tubular injury via organic anion transporter 1-mediated uptake.
AID1324531Binding affinity to BSA assessed as dissociation rate constants of the ligand-target complex at 2 mM in absence of L-tryptophan by (1)H relaxation dispersion NMR spectroscopy2016Journal of medicinal chemistry, 12-08, Volume: 59, Issue:23
Measurement of Ligand-Target Residence Times by
AID1624947Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis by measuring Kcat by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID1624946Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis by measuring Vmax by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID678998TP_TRANSPORTER: uptake in OAT1-expressing HEK293 cell2004Kidney international, Jan, Volume: 65, Issue:1
Characterization of uremic toxin transport by organic anion transporters in the kidney.
AID1324525Binding affinity to BSA assessed as binding constant at 1H-2 resonance by (1)H relaxation dispersion NMR spectroscopy2016Journal of medicinal chemistry, 12-08, Volume: 59, Issue:23
Measurement of Ligand-Target Residence Times by
AID680180TP_TRANSPORTER: inhibition of E1S uptake (E1S: 5 uM, indoxyl sulfate:500 uM) in S2 cells expressing human-OAT42003European journal of pharmacology, Apr-11, Volume: 466, Issue:1-2
Interactions of human organic anion as well as cation transporters with indoxyl sulfate.
AID681043TP_TRANSPORTER: inhibition of E1S uptake (E1S: 5 uM, indoxyl sulfate:500 uM) in S2 cells expressing human-OAT32003European journal of pharmacology, Apr-11, Volume: 466, Issue:1-2
Interactions of human organic anion as well as cation transporters with indoxyl sulfate.
AID1624944Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis using 1 U of enzyme measured after 24 hrs by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID681032TP_TRANSPORTER: uptake in OAT3-S2 cells2003European journal of pharmacology, Apr-11, Volume: 466, Issue:1-2
Interactions of human organic anion as well as cation transporters with indoxyl sulfate.
AID1324534Binding affinity to bovine trypsin assessed as 1H-CPMG relaxation dispersion data changes by (1)H relaxation dispersion NMR spectroscopy2016Journal of medicinal chemistry, 12-08, Volume: 59, Issue:23
Measurement of Ligand-Target Residence Times by
AID682171TP_TRANSPORTER: inhibition of benzylpenicillin uptake by Indoxyl sulfate at a concentration of 1000uM in Oat3-expressing oocyte cells2004The Journal of pharmacology and experimental therapeutics, Jun, Volume: 309, Issue:3
Mouse reduced in osteosclerosis transporter functions as an organic anion transporter 3 and is localized at abluminal membrane of blood-brain barrier.
AID680164TP_TRANSPORTER: uptake in OAT4-S2 cells2003European journal of pharmacology, Apr-11, Volume: 466, Issue:1-2
Interactions of human organic anion as well as cation transporters with indoxyl sulfate.
AID1324530Binding affinity to BSA assessed as 1H-CPMG relaxation dispersion data changes at 2 mM in presence of 0.06 to 1 mM L-tryptophan by (1)H relaxation dispersion NMR spectroscopy2016Journal of medicinal chemistry, 12-08, Volume: 59, Issue:23
Measurement of Ligand-Target Residence Times by
AID1324532Binding affinity to BSA assessed as dissociation rate constants of the ligand-target complex at 2 mM in presence of 0.03 mM L-tryptophan by (1)H relaxation dispersion NMR spectroscopy2016Journal of medicinal chemistry, 12-08, Volume: 59, Issue:23
Measurement of Ligand-Target Residence Times by
AID1624945Substrate activity at Helix pomatia arylsulfatase assessed as enzyme-mediated compound hydrolysis by measuring Km by UPLC-MS/MS analysis2019Bioorganic & medicinal chemistry, 03-15, Volume: 27, Issue:6
Comprehensive kinetic and substrate specificity analysis of an arylsulfatase from Helix pomatia using mass spectrometry.
AID1324519Binding affinity to BSA assessed as ligand-target residence time at 1H-2 resonance by (1)H relaxation dispersion NMR spectroscopy2016Journal of medicinal chemistry, 12-08, Volume: 59, Issue:23
Measurement of Ligand-Target Residence Times by
AID679381TP_TRANSPORTER: uptake in OAT1-S2 cells2003European journal of pharmacology, Apr-11, Volume: 466, Issue:1-2
Interactions of human organic anion as well as cation transporters with indoxyl sulfate.
AID679631TP_TRANSPORTER: uptake in Oat3-expressing HEK293 cells2004Kidney international, Jan, Volume: 65, Issue:1
Characterization of uremic toxin transport by organic anion transporters in the kidney.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (1,049)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990217 (20.69)18.7374
1990's24 (2.29)18.2507
2000's106 (10.10)29.6817
2010's456 (43.47)24.3611
2020's246 (23.45)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 59.37

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index59.37 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.32 (4.65)
Search Engine Demand Index92.07 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (59.37)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials54 (4.98%)5.53%
Trials0 (0.00%)5.53%
Reviews101 (9.32%)6.00%
Reviews0 (0.00%)6.00%
Case Studies28 (2.58%)4.05%
Case Studies0 (0.00%)4.05%
Observational18 (1.66%)0.25%
Observational0 (0.00%)0.25%
Other883 (81.46%)84.16%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]